体内活性抑制,In vivo knockdown英语短句,例句大全

体内活性抑制,In vivo knockdown
1)In vivo knockdown体内活性抑制
2)activity of inhibiting sarcoma体内抑瘤活性

英文短句/例句

1.Research of Antitumor Effect of Gene Gun-mediated DNA Vaccine pVAX1-2PFc GB Immunization in Balb/c Mice;基因枪介导pVAX1-2PFcGB融合肿瘤抗原基因疫苗小鼠体内抑瘤活性研究
2.Experimental Research on the in Vitro/in Vivo Tumor-Inhibitory Action of Skeletal Muscle Derived Tumor Suppressor;骨胳肌源性抑瘤物体内、体外抑瘤作用的实验研究
3.Study on AngiotensionⅠ-Convert Enzyme Inhibiting Activity of Corn and Soybean Peptides in vivo玉米大豆复合肽体内ACE抑制活性研究
4.Experiments Studies on Inhibitory Effects of Chimeric Molecule VEGI～+ on Human Malignant Lymphoma in Vivo;嵌合分子VEGI～+抑制人恶性淋巴瘤的体内实验研究
5.Primary Study on the Isolation of Antitumor Component from Water-caltrop;菱角中抗肿瘤活性成分的分离及体外抑瘤作用的初步研究
6.Construction of a New DNA Tumor Vaccine and Preliminary Study on Its Anti-tumor Effects新型肿瘤基因疫苗载体的构建及其抑瘤活性的初步研究
7.Stereotactic Biopsy Diagnosis for Multifocal Gliomas;立体定向活检诊断颅内多发性胶质瘤
8.The Research of Restrain by Injecting Riperygium, Wilfordii. Hook Extracted by Alcohol into the Implanted Tumors of Rats;雷公藤醇提液瘤体内注射对小鼠移植性肿瘤的抑制作用研究
9.Inhibition of K562 Cell Growth in Vitro by the Extract of Musca Domestica Iarvae工程蝇蛆体内活性物质体外抗肿瘤作用的研究
10.In vitro and in vivo evaluation of antitumor effect of resveratrol against malignant melanoma白藜芦醇对恶性黑色素瘤生长抑制作用的体外及体内研究
11.Study on the Biosynthesis, Formation and Antitumor Activity in Vitro of Exopolysaccharides Produced by Lactic Acid Bacteria;乳酸菌胞外多糖的生物合成及其组成和体外抑瘤活性研究
12.The Purification Methods of ACRP30 and the Studies of Tumor Inhibition on ES-2 in Vitro;脂联素蛋白的纯化方法及卵巢癌ES-2体外抑瘤活性研究
13.Experimental Study on the in Vivo and in Vitro Anti-tumor Effect of Swelling-dispersing Decoction;散结抗瘤方体内和体外抑瘤作用的实验研究
14.Effect of Cyclooxygenases-2 Small Interfering RNA on Gastric Adenocarcinoma Cell Line SG C-7901 in Vitro and in Vivo;RNAi抑制COX-2活性对人胃腺癌细胞系SGC-7901生长抑制的体内外研究
15.The expression product shows activity of antitumor in vivo.表达产物在体内具有一定的抗肿瘤活性。
16.Anti-tumor Principles of Asparagus Filicinus: Structure, Bioactivity and Analysis;小百部的抗肿瘤活性成分及其体内外分析
17.Antitumor Activity of 6-Fluoro-thiochromene[4,3-c]pyrazoline in Vivo6-F硫色烯并[4,3-c]吡唑啉的体内抗肿瘤活性
18.Effect of targeting IL18-EGF fused protein on the antineoplastic activity in vivo靶向IL18-EGF融合蛋白体内抗肿瘤活性研究

相关短句/例句

activity of inhibiting sarcoma体内抑瘤活性
3)in vitro inhibition activity体外抑制活性
1.The in vitro inhibition activity of the lipid-soluble epigallocatechin-3-O-gallate-4 -palmitate on ovarian cancer cells HO-8910 was investigated and compared with that of green tea polyphenols and lipophilic tea polyphenol.药理学实验考察并比较了脂溶性的表没食子儿茶素-3-O-没食子酸-4'-棕榈酸酯、水溶性的绿茶多酚和脂溶性茶多酚对人卵巢癌HO-8910细胞株的体外抑制活性。
4)in vivo Inhibition活体抑制
5)inhibitory activity抑制活性
1.Synthesis and HIV-1 reverse transcriptase inhibitory activity of 3,4-substituted quinolinone derivatives3,4-取代喹啉酮类衍生物的合成及其对HIV-1逆转录酶的抑制活性
2.Primary results showed that some of the compounds displayed potential inhibitory activity at a concentration ranging from 0.2 mmol/L时部分化合物对该酶有较好的抑制活性。
3.Various kinds of N-substituted pseudo-aminosugars derivatives,which show more potent inhibitory activity against α-glycosidase than the parent compounds,have been synthesized by chemical modification of pseudo-aminosugars.井冈霉醇胺、井冈霉胺和井冈胺等假氨基糖类物质是新型的α 糖苷酶抑制剂,对其进行化学修饰可以得到糖苷酶抑制活性更强的N 取代假氨基糖衍生物。
6)inhibiting activity抑制活性
1.Synthesis, quantitative structure-activity relationship (QSAR) study of inhibiting activity against Sphaerotheca fuliginea and molecular design of acetophenone oxime derivatives based on quantitative structure-activity relationship were performed.介绍苯乙酮肟醚类化合物的合成、瓜类白粉病抑制活性的定量构效关系(QSAR)研究以及基于QSAR研究结果的新化合物设计、合成和生测,尝试了农药先导合理设计流程在具有瓜类白粉病抑制活性的苯乙酮肟醚类化合物设计中的应用。
2.According to the result of biological experiments,2-(4,6-dimethoxy-pyrimidin-2-yloxy)-N-het/aryl-benzylamine derivatives were found to have the inhibiting activity of acetolactate synthase(ALS),and the relationship between these compounds and their activity was studied by 3D-QSAR:CoMFA and CoM-SIA.生物活性测试结果表明,2-嘧啶氧基-N-芳基苄胺类化合物对ALS具有一定的抑制活性。
3.When acted with equal proportion of Papain , the inhibiting activity of CPI lost completely; CD spectrum changed remarkably and the content of α-helix declined.水稻巯基蛋白酶抑制剂(CPI)圆二色性谱(CD)显示206nm和222nm处的双负峰,CPI分子以α 螺旋构象为主;当CPI与木瓜蛋白酶等摩尔结合后,CPI完全丧失抑制活性,复合物CD谱发生显著变化,α 螺旋含量降低。